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Specialised sourcing, R&D and distribution of raw materials

We connect manufacturers and formulators with reliable APIs, excipients, intermediates, solvents, and packaging through audited suppliers, strong quality systems, and data-driven logistics.

About

GQT Med Global is a specialist raw-materials distributor and sourcing partner serving the pharmaceutical, biopharmaceutical, nutraceutical, personal care, cosmetics, diagnostics, and medical device industries. We maintain qualified partnerships across the European Union, Middle East and North Africa (MENA), and Central and Eastern Europe (CEE), with strategic sourcing relationships spanning the EU/UK, India, China, Turkey, Israel, and the United States. We blend market intelligence, technical R&D capabilities, and quality governance to keep your development and manufacturing programmes on-specification and on-schedule.

Why GQT Med Global

We employ dual-source strategies, moving from long-list to short-list with rigorous supplier qualification. Our approach includes price discovery, allocation management, and continuous market intelligence to ensure you have access to the right materials at the right time.

Sourcing Depth

Our applications laboratory supports formulation prototypes, application testing, and scale-up programmes. We utilise Design of Experiments (DoE) and Quality by Design (QbD) principles to de-risk your development pathway and accelerate time to market.

R&D Enablement

We maintain an ISO-aligned Quality Management System with ICH Q7 awareness for active pharmaceutical ingredients and EXCiPACT-ready processes for excipients. Our distribution follows Good Distribution Practice (GDP) for active substances, ensuring product integrity.

Quality & Compliance

Every material is supported by comprehensive documentation: Certificates of Analysis (CoA), Safety Data Sheets (SDS), Technical Data Sheets (TDS), Drug Master File (DMF) and Certificate of Suitability (CEP) status, TSE/BSE declarations, GMO and allergen statements, residual solvents (ICH Q3C), elemental impurities (ICH Q3D), and REACH/CLP compliance.

Documentation-First 

Our validated temperature-controlled lanes operate at 2–8 °C and 15–25 °C with continuous data logging and real-time monitoring. We conduct route-risk assessments, maintain contingency stock, and develop alternate sourcing strategies to protect your supply continuity and business operations.

Assured Supply

What We Do

Sourcing and qualifying the right material at the right specification, then de-risking scale-up with application R&D and validated logistics. GQT Med Global serves as your strategic partner across the entire product lifecycle, from initial research and development through to commercial manufacturing and distribution.

Specialised Sourcing & Procurement

Market scanning, supplier qualification, and vendor performance monitoring. Complete documentation packages including CoA, SDS/TDS, DMF/CEP status tracking, and REACH/CLP compliance management.

R&D & Applications Laboratory

Formulation prototypes for oral, topical, and liquid systems. QbD/DoE screening, analytical method development per ICH Q2(R2), stability studies per ICH Q1A, and scale-up PPQ support.

Quality & Regulatory Support

ISO-aligned QMS with ICH Q7 awareness for APIs. Change control, CAPA, CMC support for residual solvents (Q3C), elemental impurities (Q3D), and testing via ISO/IEC 17025 partner labs.

Cold Chain & Logistics

Validated 2–8 °C and 15–25 °C lanes with data logging. WMS warehousing, FEFO/FIFO control, quarantine management, recall capabilities, and trade compliance for all major Incoterms.

Custom Synthesis & Manufacturing

Route scouting, feasibility studies, and cost modelling. Custom intermediates and key starting materials under confidentiality. Tolling, tech transfer, and impurity control strategies.

White pills arrangement

Specialised Sourcing & Distribution

APIs, Excipients & Intermediates

Comprehensive sourcing from market scanning to vendor qualification and performance monitoring. We provide complete documentation packages including CoA, SDS/TDS, specifications, and nitrosamines risk assessments. Our team tracks DMF/CEP status and manages REACH/CLP, TSE/BSE.

Syringe with Droplet

R&D & Applications Laboratory

Formulation Development

Formulation prototypes across oral solid dosage, liquids, semi-solids, and topical systems. We conduct QbD/DoE screening for excipient selection, develop and validate analytical methods per ICH Q2(R2), design stability studies following ICH Q1A, and provide scale-up and PPQ support.

Hanger with Inventory

Quality & Cold Chain Logistics

GDP-Compliant Distribution

Validated temperature-controlled lanes at 2–8 °C and 15–25 °C with continuous data logging and route-risk assessment. Warehousing with WMS, FEFO/FIFO control, quarantine management, and full recall capabilities. Trade compliance support for all major Incoterms with cargo insurance.

Scientist with Test Tubes

Ready to Accelerate Your Development Programme?

Partner with GQT Med Global for reliable pharmaceutical raw materials, expert R&D support, and validated logistics. From initial formulation through commercial manufacturing, we ensure your supply chain delivers on-specification and on-schedule.

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Efficiency

Streamlined procurement, rapid technical response, and optimised logistics accelerate your time to market and reduce costs

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Trust

Regulatory adherence, transparent documentation, and ethical sourcing practices form the foundation of every partnership

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Availability

Dual-source strategies, contingency stock, and validated cold-chain lanes ensure uninterrupted supply for your operations

Why Partner with GQT Med Global

We deliver pharmaceutical raw materials and R&D support built on three fundamental principles that ensure your success from development through commercial manufacturing.

Our Story in Numbers

98%

On-Time In-Full Delivery

Multi-site raw-material programmes delivered on schedule with complete order accuracy

0

Temperature Excursions

Validated cold-chain lanes maintaining strict product integrity from origin to destination

<72h

Technical Response Time

Standard RFQ technical pack turnaround enabling rapid decision-making and project acceleration

500+

Active Product Lines

APIs, excipients, intermediates, and specialty materials available with full regulatory documentation

Frequently asked questions

Any Question

Get in touch!

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